2,3-Dimethoxy-5-{[3-(trifluoromethyl)benzyl]sulfanyl}pyridine → 3-Hydroxy-5-{[3-(trifluoromethyl)benzyl]sulfanyl}pyridin-2(1H)-one
Reaction equation
C(SC1C=C(O)C(=O)NC=1)C1C=CC=CC=1.C[O:18][C:19]1[C:24]([O:25]C)=[CH:23][C:22]([S:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([C:35]([F:38])([F:37])[F:36])[CH:30]=2)=[CH:21][N:20]=1>>[OH:25][C:24]1[C:19](=[O:18])[NH:20][CH:21]=[C:22]([S:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[C:31]([C:35]([F:37])([F:36])[F:38])[CH:30]=2)[CH:23]=1Participants
3
Procedure
Prepared as described for 5-(benzylsulfanyl)-3-hydroxypyridin-2(1H)-one (Example 1) from 2,3-dimethoxy-5-{[3-(trifluoromethyl)benzyl]sulfanyl}pyridine (Intermediate 11).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-335e9a3a11934dff9bce55758cc28e04
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09180122B2
Reaction notes
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